🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the USA / NCT07598708
Recruiting Phase 2/3

A Study to Investigate the Effects of Cleminorexton Compared With Placebo in the Treatment of Participants With Central Disorders of Hypersomnolence

NCT07598708 · tracked via the Priya Life Science USA tracker
Sponsor
Centessa Pharmaceuticals (UK) Limited
Phase
Phase 2/3
Started
2026-05-29
Last updated
2026-09-11

Condition(s) studied

Narcolepsy Type 1Narcolepsy Type 2

Investigational drug(s) / intervention(s)

cleminorextonPlacebo

cleminorexton: Oral cleminorexton capsule

Placebo: matching placebo capsule

Study summary

Narcolepsy Type 1 (NT1) and Narcolepsy Type 2 (NT2) are rare conditions that make people feel very sleepy during the day (often referred to as excessive daytime sleepiness \[EDS\]). People living with these conditions might find it hard to stay alert and pay attention when they are at school, working, driving, or performing other daily activities.

While all conditions result in feeling sleepy, there are some differences in other common symptoms:

* NT1: People with NT1 often feel very tired during the day and experience cataplexy. Cataplexy is a sudden loss of muscle strength, which can cause someone to collapse or lose control of their muscles for a short time. This is often triggered by strong emotions, such as laughter or surprise. They may also have trouble sleeping well at night.
* NT2: People with NT2 feel sleepy during the day, just like NT1, but they do not have cataplexy.

Orexin is a protein in the brain that helps coordinate a system that plays an important role in helping people to stay awake during the daytime. Cleminorexton is designed to mimic the action of orexin. The purpose of this study is to see how safe and tolerable cleminorexton is in NT1 and NT2 and learn about what the drug does to the body. Another goal of the study is to see if cleminorexton can help people with NT1 and NT2 feel less sleepy and make other symptoms better.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Key Inclusion Criteria: * 18-70 years of age * Body Mass Index (BMI) within the range ≥ 17.0 and ≤ 45 kg/m\^2 (inclusive) * Meets the diagnostic criteria of Narcolepsy Type 1 (NT1) or Type 2 (NT2) according to International Classification of Sleep Disorders, 3rd edition, Text Revision edition (ICSD-3-TR) criteria * Is willing and able to discontinue all medications used for the treatment of narcolepsy * Is willing and able to adhere to additional protocol requirements Key Exclusion Criteria: * Medical disorder other than NT1 or NT2, that is associated with excessive daytime sleepiness (EDS) * Presence of significant cardiovascular, pulmonary, gastrointestinal, hepatic, renal, hematological, malignancy, endocrine, neurological or psychiatric disease

Primary outcome measure(s)

Trial sites (20)

FacilityCityRegionStatus
Birmingham, Alabama Birmingham Alabama Recruiting
Colorado Springs, Colorado Colorado Springs Colorado Recruiting
Brandon, Florida Brandon Florida Recruiting
Miami, Florida Miami Florida Recruiting
Miami, Florida Miami Florida Recruiting
Miami, Florida Miami Florida Recruiting
Miami, Florida Miami Florida Recruiting
Miami Lakes, Florida Miami Lakes Florida Recruiting
Orlando, Florida Orlando Florida Recruiting
Atlanta, Georgia Atlanta Georgia Recruiting
Flowood Mississippi Flowood Mississippi Recruiting
Denver, North Carolina Denver North Carolina Recruiting
Huntersville, North Carolina Huntersville North Carolina Recruiting
Cincinnati, Ohio Cincinnati Ohio Recruiting
Dublin, Ohio Dublin Ohio Recruiting
Columbia, South Carolina Columbia South Carolina Recruiting
Austin, Texas Austin Texas Recruiting
Dallas, Texas Dallas Texas Recruiting
San Antonio, Texas San Antonio Texas Recruiting
Sugar Land, Texas Sugar Land Texas Recruiting

More Centessa Pharmaceuticals (UK) Limited trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07598708 on ClinicalTrials.gov ↗ ← All trials in the USA